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pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species

Genomic Selection (GS) is the procedure whereby molecular information is used to predict complex phenotypes and it is standard in many animal and plant breeding schemes. However, only a small number of studies have been reported in horticultural crops, and in polyploid species in particular. In this...

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Autores principales: Zingaretti, María L., Monfort, Amparo, Pérez-Enciso, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385978/
https://www.ncbi.nlm.nih.gov/pubmed/30573468
http://dx.doi.org/10.1534/g3.118.200942
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author Zingaretti, María L.
Monfort, Amparo
Pérez-Enciso, Miguel
author_facet Zingaretti, María L.
Monfort, Amparo
Pérez-Enciso, Miguel
author_sort Zingaretti, María L.
collection PubMed
description Genomic Selection (GS) is the procedure whereby molecular information is used to predict complex phenotypes and it is standard in many animal and plant breeding schemes. However, only a small number of studies have been reported in horticultural crops, and in polyploid species in particular. In this paper, we have developed a versatile forward simulation tool, called polyploid Sequence Based Virtual Breeding (pSBVB), to evaluate GS strategies in polyploids; pSBVB is an efficient gene dropping software that can simulate any number of complex phenotypes, allowing a very flexible modeling of phenotypes suited to polyploids. As input, it takes genotype data from the founder population, which can vary from single nucleotide polymorphisms (SNP) chips up to sequence, a list of causal variants for every trait and their heritabilities, and the pedigree. Recombination rates between homeologous chromosomes can be specified, so that both allo- and autopolyploid species can be considered. The program outputs phenotype and genotype data for all individuals in the pedigree. Optionally, it can produce several genomic relationship matrices that consider exact or approximate genotype values. pSBVB can therefore be used to evaluate GS strategies in polyploid species (say varying SNP density, genetic architecture or population size, among other factors), or to optimize experimental designs for association studies. We illustrate pSBVB with SNP data from tetraploid potato and partial sequence data from octoploid strawberry, and we show that GS is a promising breeding strategy for polyploid species but that the actual advantage critically depends on the underlying genetic architecture. Source code, examples and a complete manual are freely available in GitHub https://github.com/lauzingaretti/pSBVB.
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spelling pubmed-63859782019-02-26 pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species Zingaretti, María L. Monfort, Amparo Pérez-Enciso, Miguel G3 (Bethesda) Software and Data Resources Genomic Selection (GS) is the procedure whereby molecular information is used to predict complex phenotypes and it is standard in many animal and plant breeding schemes. However, only a small number of studies have been reported in horticultural crops, and in polyploid species in particular. In this paper, we have developed a versatile forward simulation tool, called polyploid Sequence Based Virtual Breeding (pSBVB), to evaluate GS strategies in polyploids; pSBVB is an efficient gene dropping software that can simulate any number of complex phenotypes, allowing a very flexible modeling of phenotypes suited to polyploids. As input, it takes genotype data from the founder population, which can vary from single nucleotide polymorphisms (SNP) chips up to sequence, a list of causal variants for every trait and their heritabilities, and the pedigree. Recombination rates between homeologous chromosomes can be specified, so that both allo- and autopolyploid species can be considered. The program outputs phenotype and genotype data for all individuals in the pedigree. Optionally, it can produce several genomic relationship matrices that consider exact or approximate genotype values. pSBVB can therefore be used to evaluate GS strategies in polyploid species (say varying SNP density, genetic architecture or population size, among other factors), or to optimize experimental designs for association studies. We illustrate pSBVB with SNP data from tetraploid potato and partial sequence data from octoploid strawberry, and we show that GS is a promising breeding strategy for polyploid species but that the actual advantage critically depends on the underlying genetic architecture. Source code, examples and a complete manual are freely available in GitHub https://github.com/lauzingaretti/pSBVB. Genetics Society of America 2018-12-20 /pmc/articles/PMC6385978/ /pubmed/30573468 http://dx.doi.org/10.1534/g3.118.200942 Text en Copyright © 2019 Zingaretti et al. http://creativecommons.org/licenses/by/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software and Data Resources
Zingaretti, María L.
Monfort, Amparo
Pérez-Enciso, Miguel
pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species
title pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species
title_full pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species
title_fullStr pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species
title_full_unstemmed pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species
title_short pSBVB: A Versatile Simulation Tool To Evaluate Genomic Selection in Polyploid Species
title_sort psbvb: a versatile simulation tool to evaluate genomic selection in polyploid species
topic Software and Data Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385978/
https://www.ncbi.nlm.nih.gov/pubmed/30573468
http://dx.doi.org/10.1534/g3.118.200942
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